A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892524



Internal ID18836658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44172432..44660661hg38UCSC Ensembl
Outerchr14:44070887..44781215hg38UCSC Ensembl
Innerchr14:44641635..45129864hg19UCSC Ensembl
Outerchr14:44540090..45250418hg19UCSC Ensembl
Innerchr14:43711385..44199614hg18UCSC Ensembl
Outerchr14:43609840..44320168hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38710329
hg19710329
hg18710329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781440, essv25780950
Samples
Known GenesFSCB
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892524
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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